Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a Newα-Thalassemic Hemoglobin Variant Found in the Iberian Peninsula: Report of Six Cases-Reference-Cited by-同舟云学术

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Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a Newα-Thalassemic Hemoglobin Variant Found in the Iberian Peninsula: Report of Six Cases

Published:2012-08 Issue:6 Volume:36 Page:517-525
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Bento Celeste,Oliveira Ana Catarina,Neves Joana,Gameiro Mariline,Cunha Elizabete,Coucelo Margarida,Costa Ricardo Marques,Barbot José,Costa Emilia,Fernández-Lago Carlos,Ribeiro M. Leticia

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2012.742911

Reference22 articles.

1. Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia

2. α-Globin Genotypes in a Spanish Population

3. THE THALASSEMIA SYNDROMES: MOLECULAR CHARACTERIZATION IN THE SPANISH POPULATION

4. Molecular Basis of A-Thalassa in Portugal

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Stability of Maleimide-PEG and Mono-Sulfone-PEG Conjugation to a Novel Engineered Cysteine in the Human Hemoglobin Alpha Subunit;Frontiers in Chemistry;2021-07-26

2. Hb Plasencia [α125(H8)Leu→Arg (α2)] is a Frequent Cause ofα+-Thalassemia in the Portuguese Population;Hemoglobin;2013-01-31

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